| Approved symbol | SAMD9 |
|---|---|
| Approved name | sterile alpha motif domain containing 9 |
| HGCN ID | HGNC:1348 |
| Previous symbols | C7orf5 |
| Inheritance | |
| OMIM | 610456 |
| Chromosome | 7q21.2 |
| Panel(s) |
NGS Dementia/ALS NGS Intellectual disability NGS Mendeliome NGS Preconception panel (for consanguineous couples) NGS Primary immunodeficiency PID NGS White matter disease |
